Canonical Allele Identifier: CA357948283

Gene: PPP3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101040529G>C , CM000666.2:g.101040529G>C	GRCh38
NC_000004.11:g.101961686G>C , CM000666.1:g.101961686G>C	GRCh37
NC_000004.10:g.102180709G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_000944.5:c.1194C>G MANE Select	NP_000935.1:p.Asn398Lys
ENST00000394854.8:c.1194C>G MANE Select	ENSP00000378323.3:p.Asn398Lys
NM_000944.4:c.1194C>G	NP_000935.1:p.Asn398Lys
NM_001130691.1:c.1194C>G	NP_001124163.1:p.Asn398Lys
NM_001130691.2:c.1194C>G	NP_001124163.1:p.Asn398Lys
NM_001130692.1:c.1068C>G	NP_001124164.1:p.Asn356Lys
NM_001130692.2:c.1068C>G	NP_001124164.1:p.Asn356Lys
ENST00000323055.10:c.1068C>G	ENSP00000320580.6:p.Asn356Lys
ENST00000394853.8:c.1194C>G	ENSP00000378322.4:p.Asn398Lys
ENST00000394854.7:c.1194C>G	ENSP00000378323.3:p.Asn398Lys
ENST00000507176.5:c.900C>G	ENSP00000422990.1:p.Asn300Lys
ENST00000512215.5:c.498C>G	ENSP00000422781.1:p.Asn166Lys
XM_017008365.1:c.1158C>G	XP_016863854.1:p.Asn386Lys
XM_024454127.1:c.1044C>G	XP_024309895.1:p.Asn348Lys